Search results for "mastocytosis with associated hematologic disorder"

The MalaCard for "mastocytosis with associated hematologic disorder" has been retired.
Searching MalaCards for entries containing "mastocytosis with associated hematologic disorder"

260 hits were found for 'mastocytosis with associated hematologic disorder'

# Family MCID Name MIFTS Score
1
P MST009 Mastocytosis 56 0.633
2
P LKM002 Leukemia 71 0.585
3
P LYM118 Lymphoma 69 0.501
4
c SYS004 Systemic Mastocytosis 60 0.494
5
P MYL006 Myeloid Leukemia 66 0.390
6
P HPT021 Hepatitis 69 0.351
7
HMT002 Hematologic Cancer 64 0.336
8
c ACT073 Acute Leukemia 60 0.318
9
P LYM026 Lymphoblastic Leukemia 62 0.317
10
BNM001 Bone Marrow Cancer 51 0.312
11
MRG013 Mirage Syndrome 29 0.310
12
MYL009 Myelodysplastic Syndrome 73 0.303
13
BNC003 Bone Cancer 58 0.297
14
c CHR090 Chronic Lymphocytic Leukemia 76 0.293
15
P BCL006 B-Cell Lymphomas 65 0.289
16
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.285
17
PRM243 Primary Bone Cancer 29 0.283
18
P MLT019 Multiple Myeloma 83 0.280
19
P ART022 Arthritis 75 0.279
20
P LYM033 Lymphoproliferative Syndrome 56 0.278
21
LYM019 Lymphosarcoma 53 0.278
22
c CHR064 Chronic Monocytic Leukemia 42 0.272
23
c HYP073 Hypersensitivity Reaction Type Iv Disease 43 0.272
24
LYM024 Lymphatic System Disease 52 0.269
25
c ADL001 Adult Lymphoma 39 0.267
26
c LKM061 Leukemia, Acute Myeloid 73 0.266
27
LYM023 Lymphatic System Cancer 33 0.263
28
P OBS005 Obesity 92 0.262
29
CTN014 Cutaneous Mastocytosis 49 0.258
30
c CHR418 Chronic Leukemia 47 0.257
31
HMT018 Hematopoietic Stem Cell Transplantation 41 0.251
32
PLS009 Plasma Cell Neoplasm 48 0.250
33
MYL031 Myeloproliferative Neoplasm 58 0.248
34
SRC014 Sarcoma 66 0.243
35
P RHM011 Rheumatoid Arthritis 89 0.243
36
ACT118 Acute Non Lymphoblastic Leukemia 30 0.242
37
INC022 Inclusion-Cell Disease 46 0.241
38
LYM115 Lymphoma, Non-Hodgkin 63 0.240
39
BNS002 Bone Structure Disease 37 0.239
40
P ADN016 Adenocarcinoma 69 0.238
41
ACD009 Acid-Labile Subunit, Deficiency of 45 0.236
42
CNN005 Connective Tissue Disease 62 0.235
43
KDS001 Kid Syndrome 53 0.234
44
P BLD051 Blood Coagulation Disease 42 0.233
45
CHL071 Child Syndrome 58 0.233
46
P CLR023 Colorectal Cancer 97 0.231
47
DFF005 Diffuse Large B-Cell Lymphoma 59 0.230
48
MLN008 Melanoma 62 0.229
49
P AST005 Asthma 82 0.229
50
VSC006 Vascular Cancer 51 0.228
51
c PRM023 Pre-Malignant Neoplasm 41 0.227
52
P PNC044 Pancreatitis 61 0.226
53
P LKM068 Leukemia, Chronic Myeloid, Somatic 68 0.222
54
P HPT023 Hepatocellular Carcinoma 92 0.222
55
LYM040 Lymphoblastic Lymphoma 53 0.217
56
RFR004 Refractory Hematologic Cancer 28 0.215
57
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 32 0.215
58
P CHR562 Chronic Myelocytic Leukemia 41 0.211
59
THR024 Thrombosis 57 0.210
60
BLD053 Blood Platelet Disease 46 0.208
61
BNL002 Bone Lymphoma 32 0.207
62
P NRP001 Neuropathy 59 0.206
63
CHR285 Chronic Myelomonocytic Leukemia 56 0.203
64
P NRV006 Nervous System Cancer 60 0.203
65
P LVR013 Liver Disease 75 0.202
66
c LKM004 Leukemia, B-Cell, Chronic 24 0.201
67
P FLL037 Follicular Lymphoma 70 0.197
68
LKC003 Leukocyte Disease 43 0.197
69
P MYL005 Myelofibrosis 67 0.197
70
c LKM050 Leukemia, Chronic Lymphocytic 1 19 0.195
71
OCL009 Ocular Cancer 59 0.195
72
P OVR042 Ovarian Cancer 76 0.194
73
ALR002 Al-Raqad Syndrome 36 0.193
74
c LKM056 Leukemia, Chronic Lymphocytic 2 21 0.191
75
MNT001 Mantle Cell Lymphoma 72 0.190
76
P RNL014 Renal Cell Carcinoma 82 0.190
77
P ENC018 Encephalopathy 59 0.190
78
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.190
79
P CNN004 Connective Tissue Cancer 40 0.190
80
ORL011 Oral Cancer 56 0.188
81
PLS016 Plasma Cell Leukemia 42 0.185
82
URT039 Urticaria 57 0.185
83
c CNN010 Connective Tissue Benign Neoplasm 32 0.185
84
SKN016 Skin Disease 66 0.184
85
PRM151 Primary Bone Lymphoma 26 0.183
86
MRG003 Marginal Zone B-Cell Lymphoma 52 0.180
87
ANR040 Aneurysm 57 0.178
88
c PND001 Pain Disorder 54 0.177
89
c LKM051 Leukemia, Chronic Lymphocytic 3 19 0.176
90
P AMY004 Amyloidosis 65 0.176
91
MXD023 Mixed Cell Type Cancer 45 0.175
92
P MYP004 Myopathy 67 0.173
93
RTC005 Reticulosarcoma 48 0.172
94
P ORL007 Oral Cavity Cancer 59 0.171
95
DRM006 Dermatitis 66 0.170
96
GRF001 Graft-Versus-Host Disease, Protection Against 52 0.170
97
c FLL041 Follicular Lymphoma 1 45 0.170
98
P DRR001 Diarrhea 60 0.170
99
HML018 Homologous Wasting Disease 13 0.169
100
RTC009 Reticulum Cell Sarcoma 47 0.169
101
RFR001 Refractory Plasma Cell Neoplasm 16 0.169
102
LRN003 Learning Disability 49 0.169
103
ALN001 Aland Island Eye Disease 45 0.167
104
BRK010 Burkitt Lymphoma 69 0.166
105
PRP021 Peripheral Nervous System Neoplasm 46 0.165
106
MTH009 Mouth Disease 61 0.165
107
P INF037 Inflammatory Bowel Disease 63 0.164
108
BRT030 Birth Defects 43 0.164
109
SPL004 Splenic Marginal Zone Lymphoma 44 0.164
110
CSY001 C Syndrome 50 0.163
111
CLL014 Cll/sll 42 0.163
112
PLS025 Plasmablastic Lymphoma 46 0.162
113
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 49 0.161
114
MST017 Mast Cell Disease 50 0.161
115
LYM104 Lymphoma, Malt, Somatic 54 0.161
116
P APL001 Aplastic Anemia 75 0.161
117
PHY002 Physical Disorder 43 0.159
118
LYM012 Lymphoplasmacytic Lymphoma 44 0.159
119
SPL012 Splenic Disease 46 0.159
120
MCR004 Macroglobulinemia 50 0.156
121
DFF001 Diffuse Cutaneous Mastocytosis 43 0.155
122
LYM048 Lymphoma, Large-Cell, Immunoblastic 25 0.153
123
SPL011 Spleen Cancer 36 0.153
124
NSD001 Nose Disease 48 0.150
125
P PSR002 Psoriasis 61 0.150
126
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.149
127
P INF032 Infertility 59 0.149
128
RSP006 Respiratory System Disease 58 0.149
129
IND002 Indolent Systemic Mastocytosis 41 0.147
130
THR004 Thrombocytosis 55 0.147
131
SKN023 Skin Tag 44 0.147
132
LYM049 Lymphoma, Small Cleaved-Cell, Diffuse 29 0.146
133
P PLY018 Polycythemia 58 0.144
134
ACR041 Acromelic Frontonasal Dysostosis 45 0.142
135
URT008 Urticaria Pigmentosa 37 0.142
136
MCS002 Mucositis 55 0.141
137
WTH001 Withdrawal Disorder 37 0.141
138
P WLD002 Waldenstrom Macroglobulinemia 58 0.140
139
P ESS003 Essential Thrombocythemia 70 0.140
140
ALC007 Alcohol Dependence 63 0.140
141
P SPS003 Spastic Diplegia 52 0.140
142
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.140
143
ALL026 Allergic Hypersensitivity Disease 52 0.138
144
VND001 Vein Disease 47 0.136
145
FRB001 Farber Lipogranulomatosis 53 0.134
146
CHR563 Chronic Eosinophilic Leukemia 46 0.133
147
P ATR011 Atrial Fibrillation 66 0.132
148
GLB003 Globe Disease 32 0.131
149
HDC001 Headache 54 0.130
150
c CRN214 Coronary Heart Disease 5 22 0.130
151
GST050 Gastrointestinal System Disease 56 0.128
152
P SKN013 Skin Benign Neoplasm 43 0.128
153
P HYP098 Hypereosinophilic Syndrome 63 0.127
154
P HST010 Histiocytosis 58 0.127
155
P MSC033 Muscle Disorders 52 0.126
156
HRY003 Hairy Cell Leukemia 57 0.126
157
AGG002 Aggressive Systemic Mastocytosis 42 0.126
158
c MCR161 Macroglobulinemia, Waldenstrom 1 27 0.126
159
P HRT017 Heart Tumor 32 0.125
160
HRT007 Heart Cancer 46 0.125
161
MST002 Mast-Cell Leukemia 48 0.125
162
c MCR162 Macroglobulinemia, Waldenstrom 2 17 0.124
163
CRC006 Carcinoid Syndrome 52 0.124
164
c ADL079 Adult Heart Tumor 16 0.123
165
BND014 Bone Development Disease 40 0.121
166
ACR002 Acrocapitofemoral Dysplasia 33 0.121
167
CLN019 Colonic Disease 51 0.120
168
MSC004 Muscle Tissue Disease 34 0.118
169
SFT003 Soft Tissue Sarcoma 57 0.117
170
PMP001 Pemphigus 50 0.116
171
SML033 Small Cell Cancer of the Lung, Somatic 54 0.116
172
SKN027 Skin Conditions 43 0.115
173
c DLT002 Dilated Cardiomyopathy 76 0.114
174
P CRN178 Coronary Heart Disease 6 21 0.114
175
LYM051 Lymphomatoid Granulomatosis 47 0.114
176
P NPH012 Nephrotic Syndrome 59 0.113
177
ATY042 Atypical Chronic Myeloid Leukemia 48 0.113
178
AYM001 Ayme-Gripp Syndrome 41 0.113
179
ALP008 Alopecia 57 0.112
180
P PRT013 Portal Hypertension 60 0.110
181
DSS009 Disseminated Intravascular Coagulation 51 0.110
182
CNT018 Central Nervous System Leukemia 37 0.109
183
CHL068 Cholestasis 59 0.109
184
MDS022 Mediastinitis 41 0.106
185
SPL018 Splenomegaly 44 0.103
186
PLY125 Polycythemia Vera, Somatic 63 0.102
187
c PRM012 Primary Polycythemia 52 0.102
188
CLR030 Clear Cell Renal Cell Carcinoma 53 0.101
189
GST040 Gastric Adenocarcinoma 52 0.101
190
c AST039 Asthma 2 28 0.100
191
PHR003 Pharyngitis 56 0.099
192
SNS023 Sensory System Cancer 43 0.098
193
c HMG001 Hemoglobin C Disease 47 0.098
194
P CYS018 Cystitis 52 0.098
195
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.097
196
MST006 Mast Syndrome 43 0.097
197
HRT029 Heart Tumor of the Child 15 0.096
198
VSC009 Vascular Skin Disease 19 0.096
199
c RTN162 Retinitis Pigmentosa 2 48 0.096
200
GST019 Gastrointestinal Stromal Tumor 73 0.096
201
c AST037 Asthma 1 29 0.095
202
P MNC007 Monocytic Leukemia 55 0.093
203
ADR038 Adermatoglyphia 46 0.092
204
LNG013 Lung Lymphoma 38 0.091
205
BNF002 Bone Fracture 50 0.091
206
c THR090 Thrombocythemia 1 30 0.090
207
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.090
208
P SHR029 Short Syndrome 58 0.089
209
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.088
210
PRT018 Portal Vein Thrombosis 49 0.088
211
CRD119 Cardiac Arrest 61 0.088
212
LYM116 Lymph Node Disease 47 0.088
213
P RTN024 Retinoblastoma 74 0.088
214
P OST001 Osteopetrosis 63 0.088
215
c THR086 Thrombocythemia 3 25 0.087
216
MXD005 Mixed Connective Tissue Disease 62 0.086
217
c CRN177 Coronary Heart Disease 7 20 0.086
218
P NPH009 Nephrolithiasis 60 0.085
219
LYM020 Lymph Node Cancer 39 0.084
220
c FML303 Familial/multiple Cancer 14 0.084
221
MYL003 Myeloid Sarcoma 48 0.083
222
P EXN002 Exanthem 57 0.082
223
MXD032 Mixed Germ Cell Tumor 34 0.082
224
P CTS001 Cutis Laxa 58 0.080
225
PRN049 Paraneoplastic Pemphigus 40 0.078
226
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.077
227
GST078 Gastrointestinal Allergy 40 0.077
228
MSC072 Muscle Cancer 49 0.075
229
c JVN003 Juvenile Xanthogranuloma 44 0.074
230
MXD025 Mixed Germ Cell Cancer 31 0.073
231
P ANR002 Aniridia 64 0.071
232
HYP063 Hypersplenism 48 0.070
233
MYL015 Myeloproliferative Disorder with Eosinophilia 34 0.069
234
c HMG004 Hemoglobin D Disease 31 0.064
235
c ACT004 Acute Diarrhea 39 0.064
236
MNC006 Monoclonal Gammopathy of Uncertain Significance 44 0.063
237
ACT058 Active Peptic Ulcer Disease 43 0.061
238
CRC014 Carcinoid Tumors, Intestinal 40 0.058
239
PRM053 Primary Release Disorder of Platelets 11 0.057
240
EHR002 Ehrlichiosis 38 0.057
241
P ATX010 Ataxia Neuropathy Spectrum 30 0.057
242
c PRM149 Primary Hypereosinophilic Syndrome 38 0.056
243
c PSR017 Psoriasis 2 37 0.055
244
TNG003 Tongue Cancer 58 0.054
245
PGM003 Pigmentation Disease 39 0.054
246
PRT058 Pure Autonomic Failure 52 0.053
247
MLT001 Multiple Chemical Sensitivity 43 0.053
248
TNG004 Tongue Disease 39 0.053
249
c SML034 Small Cell Neuroendocrine Carcinoma 42 0.050
250
SML031 Small Cell Carcinoma of the Bladder 37 0.049
251
TLN003 Telangiectasis 52 0.048
252
BCL010 B-Cell Expansion with Nfkb and T-Cell Anergy 47 0.047
253
SKN021 Skin Sarcoma 25 0.046
254
OLF005 Olfactory Neuroblastoma 44 0.045
255
GST015 Gastric Small Cell Carcinoma 35 0.044
256
NTR018 Neutrophilia, Hereditary 42 0.043
257
CMP001 Composite Lymphoma 37 0.042
258
MXD027 Mixed Type Thymoma 30 0.040
259
P ACT232 Acute Necrotizing Encephalopathy 18 0.033
260
URN001 Urinary Bladder Small Cell Neuroendocrine Carcinoma 21 0.031